EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS059-00596 
Organism
Homo sapiens 
Tissue/cell
GM12878 
Coordinate
chr1:21650290-21653160 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs213024chr121650664hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr1:21650302-21650323ATTTTCTTTCTTTTTTTTTTT+6.41
JUN(var.2)MA0489.1chr1:21651121-21651135ATGACTCATTCTCC-6.04
JUN(var.2)MA0489.1chr1:21651116-21651130AAAAAATGACTCAT+7.52
Nkx2-5(var.2)MA0503.1chr1:21652787-21652798CTTGAGTGCCT-6.14
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_00105chr1:21640019-21654616Adipose_Nuclei
SE_00854chr1:21648312-21655068Adrenal_Gland
SE_01643chr1:21650385-21655084Aorta
SE_02944chr1:21650503-21654392Bladder
SE_03598chr1:21650640-21651193Brain_Angular_Gyrus
SE_03598chr1:21651214-21652589Brain_Angular_Gyrus
SE_03598chr1:21652795-21653500Brain_Angular_Gyrus
SE_04518chr1:21650430-21654343Brain_Anterior_Caudate
SE_05710chr1:21650819-21652666Brain_Cingulate_Gyrus
SE_05944chr1:21650172-21654641Brain_Hippocampus_Middle
SE_08398chr1:21650274-21654628Brain_Inferior_Temporal_Lobe
SE_08982chr1:21651888-21652526Brain_Mid_Frontal_Lobe
SE_26127chr1:21650420-21654272Duodenum_Smooth_Muscle
SE_26770chr1:21650381-21654470Esophagus
SE_28486chr1:21650385-21652524Fetal_Intestine
SE_29337chr1:21650482-21652798Fetal_Intestine_Large
SE_31433chr1:21650314-21655007Gastric
SE_39164chr1:21650503-21653287IMR90
SE_42174chr1:21650278-21654424Lung
SE_44380chr1:21650380-21654322NHDF-Ad
SE_45045chr1:21650463-21654349NHLF
SE_46660chr1:21650609-21653070Ovary
SE_47592chr1:21650567-21653016Pancreas
SE_48583chr1:21650390-21654421Right_Atrium
SE_50108chr1:21650386-21654252Sigmoid_Colon
SE_52633chr1:21650385-21654180Small_Intestine
SE_53334chr1:21650242-21653182Spleen
SE_54639chr1:21650371-21654862Stomach_Smooth_Muscle
SE_56171chr1:21650384-21653718u87
SE_65263chr1:21650278-21654762Pancreatic_islets
SE_67931chr1:21650384-21653718u87
SE_68932chr1:21650478-21654339H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr12165080621651685
chr12165078421652238
chr12165239921652754
Number: 1             
IDChromosomeStartEnd
GH01I021312chr12163897321657659
Enhancer Sequence
GAGATGGGGG CAATTTTCTT TCTTTTTTTT TTTTTTTTGA GACATAGTTT CACTCCATTG 60
CCCAGGCTGG AGTGCAATGG TGCAATCTCG GCTCACTGCA ACCTCCACCA CCCGGGTTTC 120
AAGCTATTTT CCTGCCTCAG CCTCCTTGAG TAGCTGGGAT TACAGGTATG CACCACCATG 180
CCCGGCTAAT TTTTTTGTAT TTTTAGTAGA GATGGGTTTT TGCCATGTTG GTCTGGCTGA 240
CCTCAAACTC CTGACCTCAA GTGATCCACC TGCCTCAGCC TCCCAAAGTG CTGGGATTAC 300
AGGCATGAGC CACTTCACCC GGCCTGTTTT GTTTTTAAAG AGACAAGGTC TCACTCTGTT 360
GCCCAAGCTG GAGTGCGGCC TTGACCATAG CCCATGCAGC CTCGACCATA GCTCATGCAG 420
CCTTGACCTC CTGGGCTCAA GCGATCCTCT TGCCTCAGCC TCCCAAGTAG CTGGGACTAC 480
AGATGTGCAC CACCACACCC GGGCTCATAT AGCTTCTTAA CTGGGTGGGC AGAGGAAGCA 540
GGGGGCAGAG GCCCATCCCC AAGGGAGAAA CCATCCATCA GTGCGGGACT GACAGGGACA 600
CTCCACCCAC TCAGCCCAGT GTGCTTCTGT CCAGGGAGAC TCCAACGGCT GCCACAGCTG 660
TGGTTTACTG ACTTCAGGTC TGACTGCCCT CTCCAGAGCT GCCCTAGAAT CCCTTTGTCT 720
GTGGCTGAAG TGTCCCTCAG AGCTGAGGAA CAAGTTTGGA GAGGACCAGG AGGGGCTCTC 780
CCCACCCCCG CCCCTTTCCC ACATGAAGAG AAACATTTCA GGGTTGAAAA AATGACTCAT 840
TCTCCCCAGA GAGGGCTGGA GCTGAGCTGA GTCAGGCAGA AGGAGCCCGC GGGTCACTTA 900
ATCGGCCTCC CTGCTCTGGC AGAGATGGCT CTGGGCCCCA GGAAGCCAGG GACAAATGGA 960
GGCGGAGGTG GCAGAGATAA GCAGCTAGTG GAGTGTGCCA GCCTCTCCTT CCCCAACCGA 1020
GTGTGTCACT GGGCGTCACC CAGCACTGCT CAAGTTGAAC CTGATGCAGA AGAAAAATTC 1080
CTCTGGACTT TCCTGAACGA GCTTTATGGC TGACTCACTG CCACCTGGAG CCTGCAAGAA 1140
AAGTCACAAA TCACGAAAGA AGGAGAAAAA CAGTTCTCGT TAAGCCATGT CTTCAATGGA 1200
GGTATCAGAG GTCGCCAGGA GGAAAGCACA CATGTTTTGT TGTGGGTTTC CTTCTCTAAA 1260
GAAACACGTT ACACAATAGA GGGGGGTTGA GACTGGTTGC AAAACTGCAA AATCCAATTT 1320
TGTGTACTGG ATTCAATTTC TTCATTAGCT GACACTAAAC ACAGAGACGG GGCCCTTGTG 1380
ACTAGATGAA CCATAAACTG GCTCCAGGAC CACCAACCTG GTACCTGATG GCTTGTTTCT 1440
GCTCCCCACT CTTTCCCTCC ATGCATCTTT CTCTGAGCTT CTGCTCAAGG CAGGTGCCAG 1500
GACAAGCCAG CGTCTCGAGC GGTTCCCCTT CAGCGGTGAG AAGTAACGTC ACAATTAAGG 1560
GGCAAGAGGG GCCAGAGGAC AGAACAGTGC CAGTTCCTCA TCCAGATTGA AATTTGCTTC 1620
CAGCTGCCTG TCCCCACACC AGAAAGGGCA CTCCCTGCTC CCCATGCAGG CTTCTCATCC 1680
TCTTTTGCTG GCCTCCTCCC TCCTCGCTGT CCCTGGTCTT TTTCAGCCAC AAGCAAAACA 1740
CACTCAGCCT TGAAGTCAGA TGCTCTACAG AAGCCTGCAA AAACAGAGTC AGGAGTTGTG 1800
TGGCCTTGGC CGAGTCACCT CACCTCACCA AGCCTCAGCC TCCTCACCTA TTAAATGGGG 1860
ACACAATAGG ACCCACTTCC TTGGAGCTGA CTGAGGTATG AATTGAGTCA ATGCATTCAT 1920
TGCTCAGCAC ACAGCTTAGC TCAAAGTTAA TGCTCAATAA ATTGTGGTTC CCACCTCCTG 1980
CTCCACGGAG CAGACATGAA ACAGGTACGA GAAGCAACGA GAAGGGGCGG CAGCAGAGCA 2040
TCAACACACA GGGAGTCCTG CCTACTGTCC CGACGCCACC CAGAGGCTCA AGGGGTGCCC 2100
CGGCTGCTCT CCGAAGCTGC CGGTGGCACT TTCGCCAGCC ACCTTGTTTC CAAACTTGCT 2160
GCCAGCTTCC CCTAGCGCAG TGATTTCCAC AACGGAGCTC CCGGCTGTGG GAAGGGGGCT 2220
TTCTTTGACT TGTCCTAAAA TGGCCTCACC TGGACCCAGT GGGGTGTGGG GACCAGGGGG 2280
CTGGGCCTGG ACCTATGAGC ATGTTTCCTG CCTCCTCTCA GCCCCCATCC TTCTGCCGCC 2340
CCACGTTCTC AGCCAACAAT AGCTGCTTCC CAGACTCAGC TGCCACACAG CACGAGCTCC 2400
CTGAGCAAAA ATACCCATGC GGGGGAGGGT GGGGAGGTAC AGGAGGGGCC ACAAATGGGG 2460
AGGGCTGGGA GAAGGGGTGG CAGGATCAAG CTTGTCTCTT GAGTGCCTAC TGTGTGTCAA 2520
GCTGAGAAGG GTGAAGCCCC TGGGGGTTAG AGAAACCTGG GAGACCGTGG GGTGTGTGTG 2580
TCGGGGGTGC TGGTCTCTAA GACAGCAGAG CCTCCAGTCC CCAGAGAGGG ATCAGACCCA 2640
GGTCCAGGGT CTAAGGGTGA AGAAGGGGTC CAGGGAGAAG AAGGTGCCTA AGCAGGAAGC 2700
AGGTCCTAGA ACCTAGTGAG AAAAAAGGGG GGCCTGAACC CCAAAGAGAG ATCCAAATCT 2760
TAAGGAAAAT AGGGGCTCAG GTTCGAGGAG ATGAGGTTCA TAATAGGGGG GTTATATTTC 2820
TGGTTTCAGG AGGGGGATGG TTTGGAGCAG CGTAGGGAGG TGGGGCGAGG 2870